Chemiluminescent compositions, enhancing reagents for chemiluminescence and methods for the preparation and use thereof

ABSTRACT

A enhancing reagent for enhancing chemiluminescence of 1,2-dioxetane compounds and a method for using the enhancing reagent to enhance chemiluminescence are provided, in which the enhancing reagent contains a multi-alkyl quaternary ammonium salt of Formula I. A chemiluminescent composition with a 1,2-dioxetane compound as a substrate and a kit thereof are further provided, which contain a 1,2-dioxetane compound and a multi-alkyl quaternary ammonium salt of Formula I.

RELATED APPLICATIONS

This application claims priority to Chinese Patent Application No. 201010215765.9, filed Jun. 30, 2010, for “REAGENTS FOR ENHANCING CHEMILUMINESCENCE, METHODS THEREOF, AND CHEMILUMINESCENT COMPOSITIONS,” the disclosure of which is fully incorporated herein by reference.

FIELD OF DISCLOSURE

The present disclosure relates to the field of chemiluminescence immunoassay, particularly reagents and methods for enhancing chemiluminescence of a 1,2-dioxetane compound, preparation methods and kits thereof, chemiluminescent compositions containing the enhancing reagents, preparation methods and kits thereof.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a plot of relative luminescence intensity vs. time for the chemiluminescent composition of Example 18, wherein the X-axis is time and the Y-axis is luminescence intensity;

FIG. 2 is a comparison of luminescence signals of luminescent compositions with or without the enhancing reagent in Example 19, with a commercial luminescent composition control, wherein the X-axis is time and the Y-axis is luminescence intensity;

FIG. 3 is a comparison of luminescence signals of luminescent compositions with or without the enhancing reagent in Example 20, with a commercial luminescent composition control, wherein the X-axis is time and the Y-axis is luminescence intensity; and

FIG. 4 is a comparison of luminescence signals of luminescent compositions with or without the enhancing reagent in Example 21, with a commercial luminescent composition control, wherein the X-axis is time and the Y-axis is luminescence intensity.

DETAILED DESCRIPTION OF THE DISCLOSURE

As a non-radioactive immunoassay technology, chemiluminescence immunoassays developed very quickly in the world after enzyme immunoassay (EIA), radioimmunoassay, and fluorescence immunoassay technologies. Chemiluminescence immunoassay is a microassay technology which has high sensitivity, wide detection range, simple and fast operation, stable label, and low contamination, making it a desirable quantitative immunoassay method.

Luminol, isoluminol, acridine esters, and 1,2-dioxetane compounds are used as luminescent substances in chemiluminescence immunoassays. Isoluminol and acridine esters are labeled directly and act as tracing molecules in flash-type chemiluminescent reactions. However, Luminol and the 1,2-dioxetane compounds are activated by enzymes and act as tracing molecules after enzymatic catalysis in a glow-type chemiluminescent reaction. The 1,2-dioxetane compounds are alkaline phosphatase (ALP) substrates with ultra-high sensitivity. When they contact ALP in appropriate buffers, ALP will hydrolyze them to provide strong optical signals which can be maintained over 20 hours. So, 1,2-dioxetane compounds are regarded as desirable chemiluminescent substances. Several manufacturers have developed kits where ALP is the labeling enzyme and 1,2-dioxetane compounds are ALP's substrates. These kits were used in some automatic chemiluminescence systems, for example, developed by DPC, Beckman, BioMerieux, and Olympus.

Some 1,2-dioxetane compounds such as CSPD, CDP, CDP-Star, and BZPD and luminescent compositions thereof are patented and have good luminescence and high prices. Another 1,2-dioxetane compound, 3-(2-spiroadamantane)-4-methoxy-4-(3-phosphoryloxy)phenyl-1,2-dioxetane (AMPPD), is widely known but the optical signal intensity is much weaker than that of the compounds above.

The molecular structure of AMPPD has a four-member heterocycle with a very weak —O—O— bond and a phosphate group, in which the phosphate group maintains the stability of the whole molecular structure. Normally, this compound is very stable, and is scarcely decomposed when stored at 5° C. as a solid. After catalysis by alkaline phosphatase, AMPPD is hydrolyzed at the phosphate group to form a labile intermediate. The intermediate automatically decomposes, with the four-member heterocycle with an —O—O— bond releasing a great deal of energy, thus exciting a chemiluminescent reaction, and emitting photons.

In 1989, Schaap reported a technology for enhancing the chemiluminescence of 1,2-dioxetane compounds using cetyltrimethylammonium bromide and 5-(N-tetradecanoyl)-aminofluoroescein (Clin. Chem., 35). In U.S. Pat. No. 4,959,182 and U.S. Pat. No. 5,004,565, and Chinese Patent CN89106249.1, Schaap describes methods for enhancing chemical and enzymatic triggered chemiluminescence of 1,2-dioxetane compounds by forming a micelle using cetyltrimethylammonium bromide.

U.S. Pat. No. 5,145,772 discloses that poly(vinylbenzyldimethylbenzylammonium chloride) (BDMQ) and a macromolecular substance such as serum albumin can enhance luminescence of 1,2-dioxetane compounds. U.S. Pat. No. 5,547,836 discloses that poly(vinylbenzyltrimethylammonium chloride) (TMQ) and poly(vinylbenzyltributylammonium chloride) (TBQ) are useful as enhancing reagents for luminescence of the 1,2-dioxetane compounds.

U.S. Pat. No. 5,393,469 discloses that polymeric quaternary phosphonium salt provides enhanced chemiluminescence from enzymatically triggered 1,2-dioxetane compounds.

U.S. Pat. No. 5,650,099 and Chinese Patent CN1208399A disclose that dual-cationic surfactants such as trioctylphosphinemethyl-4-tributylphosphinemethylphenyl dichloride, and fluorescent substances such as fluoroescein and hydroxypyrenesulfonic acid, provide enhanced luminescence from 1,2-dioxetane compounds.

Chinese Patent CN1719254A discloses a chemiluminescent composition including CSPD as substrate and enhancing reagents containing cetyltrimethylammonium chloride, myristoylglycerol phosphate disodium, bovine serum albumin, and octadecylamino fluoroescein.

Most of the enhancing reagents for enhancing luminescence of the 1,2-dioxetane compounds disclosed in the patents above are polymers and long-chain alkyl fluorescent substances, and they are expensive and not easily available.

Therefore, this disclosure provides a new chemiluminescent composition, a new reagent and a method for enhancing the luminescence of 1,2-dioxetane compounds.

The present disclosure relates to enhancing reagents for enhancing luminescence of 1,2-dioxetane compounds, and kits thereof, the enhancing reagents or the kits comprising at least one multi-alkyl quaternary ammonium salt having the structure of General Formula I:

wherein,

R₁ and R₂ are each independently selected from C₁₋₂₈ alkyl;

R₃ and R₄ are each independently selected from C₁₋₁₂ alkyl, and phenyl C₁₋₆ alkyl, wherein the phenyl is optionally substituted with one or more substituents selected from at least one of following: halogen, hydroxyl, sulfhydryl, cyano, nitro, alkyl, alkoxy, haloalkyl, amino, alkylamino, and amido; or

R₃ and R₄ are each independently selected from

wherein n is an integer selected from 5 to 10; and

X⁻ is a negative ion.

In a second aspect, the present disclosure relates to methods for preparing enhancing reagents for chemiluminescence of 1,2-dioxetanes, the methods comprise dissolving the components of the enhancing reagents of the present disclosure in water.

In a third aspect, the present disclosure relates to methods for enhancing chemiluminescence of 1,2-dioxetanes, the methods include adding the enhancing reagents of the present disclosure to 1,2-dioxetane solutions, or using the kits of the present disclosure.

In a fourth aspect, the present disclosure relates to chemiluminescent compositions and kits thereof, which contain 1,2-dioxetane compounds and the enhancing reagent of the present disclosure.

In a fifth aspect, the present disclosure relates to the use of a multi-alkyl quaternary ammonium salt having the structure of General Formula I in the preparation of chemiluminescent compositions.

Chemiluminescent enhancing reagents of the present disclosure have simple components and desirable enhancing effects for 1,2-dioxetanes. The chemiluminescent compositions of the present disclosure provide stable, long-lasting and greatly enhanced chemiluminescence signals and may be used in chemiluminescence immunoassays, DNA probe detection, and chemiluminescence analysis of biological membrane protein blotting. The chemiluminescent compositions of the present disclosure may be widely used in the fields of clinical diagnosis, scientific research, environmental and hygiene detection, and forensic identification.

In order to make other aspects and advantages of the present disclosure more apparent, the present disclosure is illustrated with reference to the following description and specific embodiments.

Definitions

Unless indicated otherwise, terms used herein have the following meanings.

The term “alkyl” as used herein individually or in combination with other groups refers to straight or branched alkyl groups containing 1-18 carbon atoms, such as 1-12, 1-8, and 1-6 carbon atoms. Reference to a single straight alkyl such as “n-propyl” specifically means a straight alkyl group, while reference to a single branched alkyl such as “isopropyl” specifically means a branched alkyl group. For example, “C₁₋₆alkyl” includes C₁₋₄alkyl, C₁₋₃alkyl, methyl, ethyl, n-propyl, isopropyl and tert-butyl. The same rules apply to other groups as used throughout the present specification.

The term “aryl” as used herein refers to an optionally substituted aromatic carbocyclic group, such as monocyclic or bicyclic groups having 6-12 carbon atoms in the ring moiety, for example, phenyl, biphenyl, naphthyl, substituted phenyl, substituted biphenyl, or substituted naphthyl. Preferred aryl groups are phenyl or substituted phenyl.

The term “halogen” as used herein includes fluorine, chlorine, bromine, and iodine.

The term “alkyloxy” as used herein refers to “alkyl” as defined above attached to the group —O—, wherein said “alkyl” contains 1-18 carbon atoms, for example 1-12, or alternatively 1-8, or 1-6 carbon atoms, such as methoxy, ethoxy and propoxy.

The term “benzyl” as used herein refers to —CH2-Ph group. Modification of a benzyl group by the phrase “optionally substituted with” means that the benzyl group either can exist in an unsubstituted form, or can be substituted with a suitable substituent at any suitable position. Suitable substituents include, but are not limited to, a halogen, hydroxyl, sulfhydryl, cyano, nitro, alkyl, aryl, alkoxy, heterocyclyl, haloalkyl, amino, alkylamino, amido, carboxyl, etc., so long as the compounds finally formed have the properties as contemplated by the present disclosure. In one embodiment, the benzyl group is optionally substituted with a halogen, hydroxyl, sulfhydryl, cyano, nitro or amino.

The term “a soluble salt” as used herein refers to a water soluble salt, and includes, but is not limited to, halide, sulfate, carbonate, and phosphate.

Enhancing Reagent for Chemiluminescence

In one aspect, the present disclosure provides enhancing reagents for chemiluminescence of 1,2-dioxetanes, in which the enhancing reagents contain at least one multi-alkyl quaternary ammonium salt having the structure of General Formula I:

wherein, R₁ and R₂ are each independently selected from C₁₋₂₈ alkyl; R₃ and R₄ are each independently selected from C₁₋₁₂ alkyl, and phenyl C₁₋₆ alkyl, wherein the phenyl is optionally substituted with one or more substituents selected from at least one of following: halogen, hydroxyl, sulfhydryl, cyano, nitro, alkyl, alkoxy, haloalkyl, amino, alkylamino, and amido; or R₃ and R₄ are each independently selected from

wherein n is an integer selected from 5 to 10; and X⁻ is a negative ion.

Chemiluminescence is light generated in a specific reaction of a chemical substance. Singlet molecules are excited and formed as high energy intermediates decompose in a chemical reaction, then the excited singlet molecules return to the ground state, and part of the energy is emitted in the form of luminescence. Therefore, chemiluminescent reactions include two processes: an excitation process and a luminescence process. Some molecular energy will also be dissipated in the excited state because of inter- and intra-system crossing.

The 1,2-dioxetane compounds are chemiluminescent substrates, and their structures are well-known in the art. A typical structure is as follows:

wherein R₁ is selected from at least one of alkyl, aryl, aralkyl, alkaryl, heteroalkyl, heteroaryl, cycloalkyl, heterocycloalkyl, alkyloxyalkyl, alkyloxyaryl, alkyloxyhaloalkyl, alkylalkenyl, alkylalkynyl, halogenated alkyl, alkyl alcohol, alkyl carbonitrile, alkyl amine, alkyl acid, halogenated alkyl alcohol, halogenated alkyl carbonitrile, halogenated alkyl amine, and halogenated alkyl acid; X is hydrogen or a substituent on a phenyl ring; Y is hydrogen, alkyl, acetoxyl, t-butyldimethylsilyl, a group capable of being cleaved by an enzyme, or a group capable of being cleaved by an antibody; and Z is hydrogen or a substituent on an adamantane ring.

The 1,2-dioxetane compounds used herein include, but are not limited to, 3-(2′-spiroadamantane)-4-methoxy-4-(3″-phosphoryloxy)phenyl-1,2-dioxetane (AMPPD), disodium 3-(4-methoxyspiro{1,2-dioxetane-3,2′-(5′-chloro)tricyclo[3.3.1.13,7]decan}-4-yl)phenyl phosphate (CSPD), and disodium 2-chloro-5-(4-methoxyspiro{1,2-dioxetane-3,2′-(5′-chloro)-tricyclo[3.3.1.13,7]decan}-4-yl)-1-phenyl phosphate (CDP-Star).

AMPPD can be effectively decomposed by an alkaline phosphatase, by removal of a phosphate group to form an AMPPD intermediate. The intermediate is cleaved into adamantanone and a meta-oxy methyl benzoate anion in the excited state through inter-molecular electron transfer. When the meta-oxy methyl benzoate anion transitions from the excited state to the ground state, light with a maximal wavelength of 477 nm is generated. Chemiluminescence from AMPPD catalyzed with an alkaline phosphatase can reach its peak at 15 min of reaction time, and then the optical signal strength remains relatively constant for between 15 to 60 min, with small variation. Chemiluminescence measurements may still be correct even after 12 h. AMPPD is used in a range of 0.0001-0.01 mol/L.

A person of skill in the art can understand that, based on different cleavable groups, 1,2-dioxetane compounds can be activated using different enzymes, for example, galactosidase, glucose oxidase, and catalase. In addition, Y may be chemically cleaved, to activate the 1,2-dioxetane compounds to emit light.

In chemiluminescence immunoassays, it is expected that chemical bond energy is converted into light energy as efficiently as possible, and that the generated chemiluminescence signal intensity is high and stable. The efficiency of the chemiluminescent reaction is dependent on the quantum efficiency of generating fluorescence and phosphorescence. Methods for improving the chemiluminescence intensity include: improving the quantum yield of luminescent substrate molecules, improving the enzyme activity, and stabilizing the luminescent molecules in the excited state.

In one embodiment, the enhancing reagents contain at least one multi-alkyl quaternary ammonium salt having the structure of General Formula I:

R₁ and R₂ are each independently selected from C₁₋₂₈ alkyl;

R₃ and R₄ are each independently selected from C₁₋₁₂ alkyl, and phenyl C₁₋₆ alkyl, wherein the phenyl is optionally substituted with one or more substituents selected from at least one of following: halogen, hydroxyl, sulfhydryl, cyano, nitro, alkyl, alkoxy, haloalkyl, amino, alkylamino, and amido; or

R₃ and R₄ are each independently selected from

wherein n is an integer selected from 5 to 10; and

X⁻ is a negative ion.

In one embodiment, R₁ and R₂ are identical alkyl, or R₁, R₂ and R₃ are identical alkyl.

In one embodiment, when R₃ is selected from C₁₋₈ alkyl, R₄ is selected from C₁₋₁₂ alkyl, and phenyl C₁₋₆ alkyl, wherein the phenyl is optionally substituted with one or more substituents selected from at least one of following: halogen, hydroxyl, sulfhydryl, cyano, nitro, alkyl, alkoxy, haloalkyl, amino, and alkylamino, or alternatively, R₄ is selected from C₁₋₈ alkyl or benzyl.

In one embodiment, when R₃ and R₄ are selected from

the n of R₃ and R₄ are identical integers.

In one embodiment, X⁻ is selected from halide ions, ClO₄ ⁻, PF₆ ⁻, CF₃SO₃ ⁻, BF₄ ⁻, acetate, and p-toluene sulfonate anions.

In one embodiment, a compound of the present disclosure is selected from Compound-1, Compound-2, Compound-3, Compound-4, Compound-5 and Compound-6:

While not being bound by theory, it is believed that the surfactants used in the embodiments of the present disclosure may form micelles in a solution, whose micro environment is non-aqueous. In the non-aqueous environment, the chemiluminescent reaction efficiency and quantum yield improve. Meanwhile, the surfactants may be conducive to the fluorescent molecules moving close to the chemiluminescent substrate molecules, allowing light energy transfer to occur once the chemiluminescence reaction starts. The quantum yield of the fluorescent molecules is much greater than that of the chemiluminescent molecules, thus enhancing the optical signal. The multi-alkyl quaternary ammonium salt is generally used at a concentration of 0.1 g/L to 10 g/L, for example 1 g/L to 10 g/L.

The enhancing reagents according to the embodiments of the present disclosure may further include fluorescent agents, for example, fluorescein sodium, Rhodamine B, and Rhodamine 6G. The fluorescent agents will emit another kind of fluorescence after receiving light energy from the luminescent substance. The quantum yield of fluoroescein is far greater than that of the chemiluminescent substance, so the quantum yield of the luminescent substance may indirectly improve. For example, fluorescein sodium (9-(o-carboxyphenyl)-6-hydroxy-3H-xanthene-3-ketone disodium) is a water soluble fluorescent agent, and has an excitation and emission wavelength of 494 nm and 518 nm respectively. The quantum yield of fluorescein sodium is up to 0.97. Similarly, Rhodamine series fluorescent agents also have a very high fluorescence quantum yield. The fluorescent agent is used at concentration of about 0.1 mg/L to about 1 g/L.

The enhancing reagents of the present disclosure may further contain a buffer, for maintaining the pH of the reaction system. Appropriate buffers include a carbonate buffer, a diethanolamine buffer, 2-amino-2-methyl-1-propanol, and so on. When luminescence of a chemiluminescent substance is triggered by cleavage of the phosphate group, an appropriate buffer may be a 2-amino-2-methyl-1-propanol buffer system. For example, in a reaction process where phosphate groups are cleaved by catalysis of alkaline phosphatase, 2-amino-2-methyl-1-propanol may be a phosphate receptor in phosphotransfer, so as to improve the catalytic effect of ALP. As for the alkaline phosphatase system, the most suitable pH for reaction may range from about 9 to about 10. The buffer may be used at a concentration of about 10 to about 500 mM.

The enhancing reagents of the present disclosure may further contain magnesium ions, which are from soluble salts containing magnesium ions, for example, magnesium sulfate, magnesium acetate, magnesium chloride, and other salts from which magnesium ions can be dissociated in solution. When a 1,2-dioxetane compound containing a phosphate group is used as a chemiluminescent substrate, the phosphate group can be hydrolyzed by alkaline phosphatase, thus producing chemiluminescence. In this case, the addition of magnesium ions can activate alkaline phosphatase, thereby improving the catalytic performance of alkaline phosphatase for the hydrolysis reaction. The magnesium ions are used at a concentration range from about 0.001 to about 0.01 mol/L.

The enhancing reagents of the present disclosure may further include a preservative, which facilitates the preservation and long-term storage of the reagent. There is no limitation to the type of the preservative, and commercially available preservatives such as Proclin300, sodium azide, Kathon, and Gentamicin may be used. The preservatives may be used at any concentration which will not influence the chemiluminescent reaction and the activity of alkaline phosphatase.

To prepare the chemiluminescent compositions according to the embodiments of the present disclosure, the components in the chemiluminescent compositions above are dissolved in pure water, optionally adjusted to a desired pH and brought up to the final volume with water. The pH may be adjusted according to the conditions required for activating the substrate. For example, if the substrate is activated by an alkaline phosphatase, the pH of chemiluminescent compositions may be adjusted to the range of about 9 to about 10.

The enhancing reagent according to the embodiments of the present disclosure may be made into a kit by individually packaging the components of the chemiluminescent composition into a multi-package system. In other embodiments, some components may be combined in one container, while the others are stored in separate containers to form a multi-package system. Alternatively, the components may be mixed, and then packaged as a single mixture.

Method for Enhancing Chemiluminescence

The present disclosure further provides a method for enhancing luminescence of 1,2-dioxetane compounds, which includes adding the chemiluminescent enhancing reagents or one or more components of kits of the present disclosure to a solution containing 1,2-dioxetane compounds.

Chemiluminescent Compositions, and Preparation Method and Kits Thereof

The present disclosure further provides chemiluminescent compositions, which contain 1,2-dioxetane compounds and the enhancing reagents of the present disclosure.

The chemiluminescent composition according to the embodiments of the present disclosure may be made into a kit by individually packaging the components of the chemiluminescent composition into a multi-package system. In other embodiments, some components may be combined in one container, while the others are stored in separate containers to form a multi-package system. Alternatively, the components may be mixed, and then packaged as a single mixture. According to different detection uses, the kit may further include corresponding enzyme reagents, labeled enzyme reagent, a solid-phase antibody or a manual which instructs the operator.

Use of Multi-Alkyl Quaternary Ammonium Salt Having a Structure of Formula I in Preparation of Chemiluminescent Compositions

The present disclosure provides for the use of a multi-alkyl quaternary ammonium salt having the structure of General Formula I in the preparation of chemiluminescent compositions. The multi-alkyl quaternary ammonium salt of the present disclosure enhances the chemiluminescence of substances such as 1,2-dioxetane compounds. Moreover, most of these salts are commercially available, inexpensive, and suitable for production of chemiluminescent compositions on a large scale.

EXAMPLES

The present disclosure will be further described with references to the following particular examples. These examples are intended only to be illustrative, but not to limit the scope of the present disclosure in any sense.

Unless otherwise indicated, all of chemical reagents used in the examples were analytic pure, and supplied from Sigma-Aldrich Company. The chemiluminescence analyzer is a BHP9507 chemiluminescence analyzer supplied from Beijing Hamamatsu Photon Techniques Inc.

Examples 1 to 17

A basic luminescent composition was formulated with ultra-pure water as follows:

2-amino-2-methyl-1-propanol 200 mM AMPPD 0.5 mM MgCl₂ 5 mM Proclin 300 0.5 g/L pH was adjusted with HCl to 9.5

Appropriate amounts of components other than AMPPD were weighed, dissolved into ultra-pure water, pH adjusted, and adjusted to final volume with water. AMPPD was then added and dissolved, to obtain the basic luminescent composition in which the final concentrations of the components were as shown in the table above. Components of the respective enhancing reagent were added to the basic luminescent composition to formulate the chemiluminescent compositions of Example 1-17 (see Table 1).

100 μl of the chemiluminescent composition from each example was added to 50 μl of a 1 ng/mL solution of alkaline phosphatase. Chemiluminescence intensity (RLU) was measured by a chemiluminescence analyzer and the fold increase in RLU was calculated for each chemiluminescent composition versus the basic luminescent composition. As shown in examples 2 to 9 of Table 1, the multi-alkyl quaternary ammonium salt used alone enhances chemiluminescence from the chemiluminescent composition; the effect was similar to that of the fluorescent agent used alone. Examples 10 to 17 of Table 1 also show that the multi-alkyl quaternary ammonium salt and the fluorescent agent act synergistically, significantly enhancing the luminescence signal of AMPPD.

TABLE 1 Chemiluminescent compositions of Examples 1-17 and intensity duration of chemiluminescence from AMPPD Luminescence Fold Enhancing component(s) added to intensity Increase Example basic luminescent composition (RLU) in RLU  1 No 7070 1.0  2 5 mg/L fluorescein Sodium 53025 7.5  3 1 mg/L Rhodamine 6 G 36764 5.2  4 10 g/L Compound-1 (didodecyl 31108 4.4 dimethyl ammonium chloride)  5 1 g/L Compound-5 (didodecyl 38885 5.5 polyoxyethylene ether ammonium chloride)  6 0.1 g/L Compound-2 (dioctadecyl 41006 5.8 dimethyl ammonium chloride)  7 1 g/L Compound-6 (dioctadecyl 31815 4.5 polyoxyethylene ether ammonium chloride)  8 1 g/L Compound-3 (dioctadecyl 47369 6.7 methyl benzyl ammonium bromide)  9 1 g/L Compound-4 (methyltrioctyl 68579 9.7 ammonium chloride) 10 5 g/L Compound-4 (methyltrioctyl 1063328 150.4 ammonium chloride), 5 mg/L fluorescein sodium 11 10 g/L Compound-4 (methyltrioctyl 851935 120.5 ammonium chloride), 5 mg/L fluorescein sodium 12 0.1 g/L Compound-4 (methyltrioctyl 674478 95.4 ammonium chloride), 5 mg/L Rhodamine 6 G 13 10 g/L Compound-4 (methyltrioctyl 637007 90.1 ammonium chloride), 5 mg/L Rhodamine 6 G 14 5 g/L Compound-1 (didodecyl 358449 50.7 dimethyl ammonium chloride), 5 mg/L fluorescein sodium 15 5 g/L Compound-5 (didodecyl 568428 80.4 polyoxyethylene ether ammonium chloride), 5 mg/L fluorescein sodium 16 5 g/L Compound-2 (dioctadecyl 425614 60.2 dimethyl ammonium chloride), 5 mg/L fluorescein sodium 17 5 g/L Compound-3 (dioctadecyl 391678 55.4 dimethyl ammonium bromide), 5 mg/L fluorescein sodium

Example 18

Referring to the method of Example 1, a chemiluminescent composition was prepared as follows:

2-amino-2-methyl-1-propanol 200 mM AMPPD 0.5 mM MgCl₂ 5 mM Compound-4 (methyltrioctyl ammonium chloride) 5 g/L Fluorescein Sodium 5 mg/L Proclin 300 0.5 g/L pH was adjusted with HCl to 9.5

100 μl of the chemiluminescent composition was added to 50 μl of a 1 ng/mL solution of alkaline phosphatase. Chemiluminescence intensity was measured by a chemiluminescence analyzer, and a chemiluminescent intensity-time curve was plotted. The results are shown in FIG. 1, which demonstrates that the luminescence signal of the chemiluminescent composition of the present disclosure is stable and long lasting.

Example 19 AMPPD+Enhancing Reagent

Referring to the method of Example 1, a chemiluminescent composition was formulated with ultra-pure water as follows:

2-amino-2-methyl-1-propanol 200 mM AMPPD 0.5 mM MgCl₂ 5 mM Compound-4 (methyltrioctyl ammonium chloride) 5 g/L Fluorescein Sodium 5 mg/L Proclin 300 0.5 g/L pH was adjusted with HCl to 9.5

100 μl of the chemiluminescent composition was added to 20 μl of a 1 ng/mL solution of alkaline phosphatase. Chemiluminescence intensity was measured by a chemiluminescence analyzer. A commercial chemiluminescent composition, Access Substrate (Beckman), was also measured as a control for comparison. The results are shown in FIG. 2, which demonstrates that the enhancing reagent of the present disclosure enhances the luminescence signal of AMPPD, and that the performance of the chemiluminescent composition is similar to that of Access Substrate (Beckman).

Example 20 CSPD+Enhancing Reagent

Referring to the method of Example 1, a chemiluminescent composition was prepared with ultra-pure water as follows:

2-amino-2-methyl-1-propanol 200 mM CSPD 0.25 mM MgCl₂ 5 mM Compound-4 (methyltrioctyl ammonium chloride) 5 g/L Fluorescein Sodium 5 mg/L Proclin 300 0.5 g/L pH was adjusted with HCl to 9.5

100 μl of the chemiluminescent composition was added to 20 μl of a 1 ng/mL solution of alkaline phosphatase. Chemiluminescence intensity was measured by a chemiluminescence analyzer. A commercial chemiluminescent composition, CSPD & Sapphire-II (Tropix), was also measured as a control for comparison. The results are shown in FIG. 3, which demonstrates that the enhancing reagent of the present disclosure enhances the luminescence signal of CSPD, and that the performance of the chemiluminescent composition is similar to that of CSPD & Sapphire-II (Tropix).

Example 21 CDP-Star+Enhancing Reagent

Referring to the method of Example 1, a chemiluminescent composition was prepared with ultra-pure water as follows:

2-amino-2-methyl-1-propanol 200 mM CDP-Star 0.25 mM MgCl₂ 5 mM Compound-4 (methyltrioctyl ammonium chloride) 5 g/L Fluorescein Sodium 5 mg/L Proclin 300 0.5 g/L pH was adjusted with HCl to 9.5

100 μl of the chemiluminescent composition was added to 20 μl of a 1 ng/mL solution of alkaline phosphatase. Chemiluminescence intensity was measured by a chemiluminescence analyzer. A commercial chemiluminescent composition, CSPD & Sapphire-II (Tropix), was also measured as a control for comparison. The results are shown in FIG. 4, which demonstrates that the enhancing reagent of the present disclosure enhances the luminescence signal of CDP-Star, and that the performance of the chemiluminescent composition is similar to that of CSPD & Sapphire-II (Tropix).

It can be seen from the examples above that, the multi-alkyl quaternary ammonium salts demonstrate good chemiluminescent enhancing effects for 1,2-dioxetane compounds, as well as unexpected synergistic enhancing effects in combination with fluorescent agents. Chemiluminescent compositions containing the multi-alkyl quaternary ammonium salts can generate strong luminescence signals, thereby improving the detection sensitivity of a diagnosis kit.

The data, figures, instruments, reagents and steps herein should be understood to be illustrative, but not restrictive. Although the present disclosure was described with references to the above concrete embodiments, many modifications and variances will be apparent to skilled persons in the art. All the modifications and variances also fall within the spirit and scope of the disclosure. 

What is claimed is:
 1. A method for enhancing the chemiluminescence of 1,2-dioxetane compounds, the method comprising: providing at least one aliphatic multi-alkyl quaternary ammonium salt having the structure of General Formula I:

wherein: R₁ and R₂ are each independently selected from C₈₋₂₈ alkyl; R₃ and R₄ are each independently selected from C₁₋₁₂ alkyl; or R₃ and R₄ are each independently selected from

wherein n is an integer selected from 5 to 10; and X⁻ is a negative ion; and mixing the multi-alkyl quaternary ammonium salt with a 1,2-dioxetane compound.
 2. The method of claim 1, wherein R₁ and R₂ are identical alkyl, or R₁, R₂ and R₃ are identical alkyl.
 3. The method of claim 1, wherein when R₃ is selected from C₁₋₈ alkyl, R₄ is selected from C₁₋₁₂ alkyl.
 4. The method of claim 1, wherein when R₃ is selected from C₁₋₈ alkyl, R₄ is selected from C₁₋₈ alkyl.
 5. The method of claim 1, wherein when R₃ and R₄ are selected from

n of R₃ and R₄ are identical integers.
 6. The method of claim 1, wherein X⁻ is selected from halide ions, ClO₄ ⁻, PF₆ ⁻, CF₃SO₃ ⁻, BF₄ ⁻, acetate, or p-toluene sulfonate anions.
 7. The method of claim 1, wherein the multi-alkyl quaternary ammonium salt compound is selected from at least one of: didodecyl dimethyl ammonium halide, dioctadecyl dimethyl ammonium halide, didodecyl polyoxyethylene ether ammonium halide, dioctadecyl polyoxyethylene ether ammonium halide, or a combination thereof.
 8. The method of claim 1, further comprising dissolving the multi-alkyl quaternary ammonium salt and the 1,2-dioxetane compound in water, wherein the concentration of the multi-alkyl quaternary ammonium salt is in a range of between about 0.1 g/L and about 10 g/L.
 9. The method of claim 1, further comprising dissolving the multi-alkyl quaternary ammonium salt and the 1,2-dioxetane compound in water, wherein the concentration of the multi-alkyl quaternary ammonium salt is in a range of between about 1 g/L and about 10 g/L.
 10. The method of claim 1, further comprising mixing the multi-alkyl quaternary ammonium salt and the 1,2-dioxetane compound with a fluorescent agent.
 11. The method of claim 1, further comprising mixing the multi-alkyl quaternary ammonium salt and the 1,2-dioxetane compound with at least one of: 2-amino-2-methyl-1-propanol or a magnesium ion or both.
 12. A method for enhancing the chemiluminescence of 1,2-dioxetane compounds, the method comprising: providing at least one multi-alkyl quaternary ammonium salt having the structure of General Formula I:

wherein: R₁ and R₂ are each independently selected from C₈₋₂₈ alkyl; R₃ and R₄ are each independently selected from C₁₋₁₂ alkyl; phenyl C₁₋₆ alkyl, wherein the phenyl is optionally substituted with one or more substituents selected from at least one of: halogen, hydroxyl, sulfhydryl, cyano, nitro, alkyl, alkoxy, haloalkyl, amino, alkylamino, or amido; or

wherein n is an integer selected from 5 to 10; and X⁻ is a negative ion; mixing the multi-alkyl quaternary ammonium salt with a 1,2-dioxetane compound having the following structure:

wherein R₁ is selected from at least one of alkyl, aryl, aralkyl, alkaryl, heteroalkyl, heteroaryl, cycloalkyl, heterocycloalkyl, alkyloxyalkyl, alkyloxyaryl, alkyloxyhaloalkyl, alklalkenyl, alkylalkynyl, halogenated alkyl, alkyl alcohol, alkyl carbonitrile, alkyl amine, alkyl acid, halogenated alkyl alcohol, halogenated alkyl carbonitrile, halogenated alkyl amine, and halogenated alkyl acid; X is hydrogen or a substituent on a phenyl ring; Y is hydrogen, alkyl, acetoxyl, t-butyldimethylsilyl, a group capable of being cleaved by an enzyme, or a group capable of being cleaved by an antibody; and Z is hydrogen or a substituent on an adamantane ring; and dissolving the multi-alkyl quaternary ammonium salt and the 1,2-dioxetane compound in water, wherein the concentration of the multi-alkyl quaternary ammonium salt is in a range of between about 1 g/L to about 10 g/L.
 13. The method of claim 12, wherein the R₁ and R₂ of the multi-alkyl quaternary ammonium salt are identical alkyl, or the R₁, R₂ and R₃ of the multi-alkyl quaternary ammonium salt are identical alkyl.
 14. The method of claim 12, wherein when the R₃ of the multi-alkyl quaternary ammonium salt is selected from C₁₋₈ alkyl, the R₄ of the multi-alkyl quaternary ammonium salt is selected from C₁₋₁₂ alkyl, or phenyl C₁₋₆ alkyl, wherein the phenyl is optionally substituted with one or more substituents selected from at least one of: halogen, hydroxyl, sulfhydryl, cyano, nitro, alkyl, alkoxy, haloalkyl, amino, or alkylamino.
 15. The method of claim 12, wherein when the R₃ of the multi-alkyl quaternary ammonium salt is selected from C₁₋₈ alkyl, the R₄ of the multi-alkyl quaternary ammonium salt is selected from C₁₋₈ alkyl or benzyl.
 16. The method of claim 12, wherein the multi-alkyl quaternary ammonium salt compound is selected from at least one of: didodecyl dimethyl ammonium halide, dioctadecyl dimethyl ammonium halide, dioctadecyl methyl benzyl ammonium halide, didodecyl polyoxyethylene ether ammonium halide, dioctadecyl polyoxyethylene ether ammonium halide, or a combination thereof. 